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HCID 9794351, 화합물 → 5,6,7,8-Tetrahydro-1,3-dimethyl-4H-cyclohepta[c]thiophen-4-one

HRID 1636571
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HRID 1636571 반응식
[CH3:1][C:2]1[S:3][C:4]([CH3:14])=[CH:5][C:6]=1[CH2:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=O>O>[CH3:1][C:2]1[S:3][C:4]([CH3:14])=[C:5]2[C:11](=[O:13])[CH2:10][CH2:9][CH2:8][CH2:7][C:6]=12
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참가 물질

3

반응물 1

HCID 9794351HCID 9794351, 화합물

생성물 1

HCID 102197935,6,7,8-Tetrahydro-1,3-dimethyl-4H-cyclohepta[c]thiophen-4-one수율 73%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-(2,5-Dimethyl-3-thiophenyl)pentanoic acid (12 g, 56.6 mmol) is heated in 30 g of polyphosphoric acid at 140° C. for 2 hr. After the reaction mixture is cooled to room temperature, water is added to dissolve the residual PPA. The mixture is then extracted with ether and the ether layer is washed with water, aqueous NaOH and again with water. The ether layer is then dried over sodium sulfate and the solvent evaporated under reduced pressure to yield 1,3-dimethyl-5,6,7,8-tetrahydro-4 H-cyclohepta[1,2-c]thiophen-4-one as a dark oil (8 g, 73%). 1H NMR (CDCl3) 2.70 (t, J=6.0 Hz, 2 H), 2.64 (dd, J=5.0, 7.0 Hz, 2 H), 2.55 (s, 3 H), 2.28 (s, 3 H), 1.79 (m, 4 H).

후처리

  • dissolutionto dissolve the residual PPA
  • extractionThe mixture is then extracted with ether
  • washthe ether layer is washed with water, aqueous NaOH and again with water
  • dry with materialThe ether layer is then dried over sodium sulfate
  • customthe solvent evaporated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-92179e63157d4f6c8787df60c340245a
    출처 데이터셋
    uspto-grants-2000_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06034252

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